Multiple interval mapping for quantitative trait loci

被引:1
作者
Kao, CH [1 ]
Zeng, ZB
Teasdale, RD
机构
[1] Acad Sinica, Inst Stat Sci, Taipei 11529, Taiwan
[2] N Carolina State Univ, Dept Stat, Program Stat Genet, Raleigh, NC 27695 USA
[3] Forbio Res Pty Ltd, Toowong, Qld 4066, Australia
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A new statistical method for mapping quantitative trait loci (QTL), called multiple interval mapping (MIM), is presented. It uses multiple marker intervals simultaneously to fit multiple putative QTL directly in the model for mapping QTL. The MIM model is based on Cockerham's model for interpreting genetic parameters and the method of maximum likelihood for estimating genetic parameters. With the MIM approach, the precision and power of QTL mapping could be improved. Also, epistasis between QTL, genotypic values of individuals, and heritabilities of quantitative traits can be readily estimated and analyzed. Using the MIM model, a stepwise selection procedure with likelihood ratio test statistic as a criterion is proposed to identify QTL. This MIM method was applied to a mapping data set of radiata pine on three traits: brown cone number, tree diameter, and branch quality scores. Based on the MIM result, seven, six, and five QTL were detected for the three traits, respectively. The detected QTL individually contributed from similar to 1 to 27% of the total genetic variation. Significant epistasis between four pairs of QTL in two traits was detected, and the four pairs of QTL contributed similar to 10.38 and 14.14% of the total genetic variation. The asymptotic variances of QTL positions and effects were also provided to construct the confidence intervals. The estimated heritabilities were 0.5606, 0.5226, and 0.3630 for the three traits, respectively. With the estimated QTL effects and positions, the best strategy of marker-assisted selection for trait improvement for a specific purpose and requirement can be explored. The MIM FORTRAN program is available on the worldwide web (http://www,stat.sinica.edu.tw/similar to chkao/).
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页码:1203 / 1216
页数:14
相关论文
共 48 条
[1]  
AITKEN KS, 1997, FRI B, V203, P337
[2]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[3]  
[Anonymous], 1990, SUBSET SELECTION REG, DOI DOI 10.1007/978-1-4899-2939-6
[4]  
ATKINSON AC, 1980, BIOMETRIKA, V67, P413, DOI 10.1093/biomet/67.2.413
[5]   INTERVAL MAPPING IN THE ANALYSIS OF NONADDITIVE QUANTITATIVE TRAIT LOCI [J].
CARBONELL, EA ;
GERIG, TM ;
BALANSARD, E ;
ASINS, MJ .
BIOMETRICS, 1992, 48 (01) :305-315
[6]  
CHURCHILL GA, 1994, GENETICS, V138, P967
[7]  
DARVASI A, 1993, GENETICS, V134, P943
[8]   MAXIMUM LIKELIHOOD FROM INCOMPLETE DATA VIA EM ALGORITHM [J].
DEMPSTER, AP ;
LAIRD, NM ;
RUBIN, DB .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-METHODOLOGICAL, 1977, 39 (01) :1-38
[9]  
DOERGE RW, 1996, GENETICS, V142, P284
[10]  
Draper N. R., 1966, APPL REGRESSION ANAL